pH- and thermo-sensitive MTX-loaded magnetic nanocomposites: synthesis, characterization, and in vitro studies on A549 lung cancer cell and MR imaging

Drug Dev Ind Pharm. 2018 Mar;44(3):452-462. doi: 10.1080/03639045.2017.1397686. Epub 2017 Nov 14.

Abstract

In the current study, we proposed a facile method for fabrication of multifunctional pH- and thermo-sensitive magnetic nanocomposites (MNCs) as a theranostic agent for using in targeted drug delivery and magnetic resonance imaging (MRI). To this end, we decorated Fe3O4 magnetic nanoparticles (MNPs) with N,N-dimethylaminoethyl methacrylate (DMAEMA) and N-isopropylacrylamide (NIPAAm), best known for their pH- and thermo-sensitive properties, respectively. We also conjugated mesoporous silica nanoparticles (MSNs) to polymer matrix acting as drug container to enhance the drug encapsulation efficacy. Methotroxate (MTX) as a model drug was successfully loaded in MNCs (M-MNCs) via surface adsorption onto MSNs and electrostatic interaction between drug and carrier. The pH- and temperature-triggered release of MTX was concluded through the evaluation of in vitro release at both physiological and simulated tumor tissue conditions. Based on in vitro cytotoxicity assay results, M-MNCs significantly revealed higher antitumor activity compared to free MTX. In vitro MR susceptibility experiment showed that M-MNCs relatively possessed high transverse relaxivity (r2) of about 0.15 mM-1·ms-1 and a linear relationship between the transverse relaxation rate (R2) and the Fe concentration in the M-MNCs was also demonstrated. Therefore, the designed MNCs can potentially become smart drug carrier, while they also can be promising MRI negative contrast agent.

Keywords: MRI contrast agent; Theranostic nanomedicine; dual-responsive drug delivery; lung cancer; magnetic nanoparticles; methotrexate.

MeSH terms

  • A549 Cells
  • Acrylamides / chemistry
  • Cell Line, Tumor
  • Drug Carriers / chemistry
  • Drug Delivery Systems / methods
  • Humans
  • Hydrogen-Ion Concentration
  • Lung Neoplasms / drug therapy*
  • Magnetic Resonance Imaging / methods
  • Methacrylates / chemistry
  • Methotrexate / administration & dosage*
  • Methotrexate / chemistry*
  • Nanocomposites / chemistry*
  • Nanoparticles / administration & dosage
  • Nanoparticles / chemistry
  • Polyethylene Glycols / chemistry
  • Polymers / chemistry
  • Silicon Dioxide / chemistry

Substances

  • Acrylamides
  • Drug Carriers
  • Methacrylates
  • Polymers
  • Polyethylene Glycols
  • Silicon Dioxide
  • N-isopropylacrylamide
  • 2-(dimethylamino)ethyl methacrylate
  • Methotrexate